Trifluoroacetic acid → HCID 13752778, compound
Reaction equation
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C@H:7]([CH2:9][C:10]([NH:12][C@H:13]([C:15]([NH:17][C@H:18]([C@H:23]([CH2:25][C:26]([O:28][CH3:29])=[O:27])[OH:24])[CH2:19][CH:20]([CH3:22])[CH3:21])=[O:16])[CH3:14])=[O:11])[OH:8])[CH2:3][CH:4]([CH3:6])[CH3:5].[C:37]([OH:43])([C:39]([F:42])([F:41])[F:40])=[O:38]>>[NH2:1][C@H:2]([C@H:7]([CH2:9][C:10]([NH:12][C@H:13]([C:15]([NH:17][C@H:18]([C@H:23]([CH2:25][C:26]([O:28][CH3:29])=[O:27])[OH:24])[CH2:19][CH:20]([CH3:21])[CH3:22])=[O:16])[CH3:14])=[O:11])[OH:8])[CH2:3][CH:4]([CH3:5])[CH3:6].[F:40][C:39]([C:37]([OH:43])=[O:38])([F:42])[F:41]Participants
3
Procedure
200 mg of Boc-Sta-Ala-Sta-OMe are treated with 3.5 ml of TFA at 0° C. The mixture is stirred for 20 min at RT. Then, after concentration in vacuo, the oily residued is extracted by successively adding and concentrating anhydrous ether. This gives a white solid.
Workup
- concentrationThen, after concentration in vacuo
- extractionthe oily residued is extracted
- additionby successively adding
- concentrationconcentrating anhydrous ether
- customThis gives a white solid
Sources & evidence
- ORD record
- ord-950452a3702b49b9843988c81d3b8a17
- Source dataset
- uspto-grants-1988_05
- Patent number
- US04746648
Reaction notes
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